FDA recall D-1056-2017

Product

Famotidine Tablets USP, 20 mg, 100 count bottles, Rx only, Manufactured For: TEVA PHARMACEUTICALS USA, Sellersville, PA --- NDC 0172-5728-60

Reason for recall

Failed Tablet/Capsule Specification; out of specification for tablet weight

Distribution

Nationwide

Key facts

Status

Terminated

Initiation date

2017-07-24

Report date

2017-08-09

Termination date

2018-01-31

Voluntary/Mandated

Voluntary: Firm initiated

Location

North Wales, PA, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-1056-2017